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A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Assess The Efficacy, Safety, and Tolerability of VK2809 Administered for 12 Weeks Followed by a 4-Week Off-Drug Phase in Patients With Primary Hypercholesterolemia and Non-Alcoholic Fatty Liver Disease

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Trial Profile

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Assess The Efficacy, Safety, and Tolerability of VK2809 Administered for 12 Weeks Followed by a 4-Week Off-Drug Phase in Patients With Primary Hypercholesterolemia and Non-Alcoholic Fatty Liver Disease

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 15 Oct 2020

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At a glance

  • Drugs VK 2809 (Primary)
  • Indications Hypercholesterolaemia; Non-alcoholic fatty liver disease
  • Focus Proof of concept; Therapeutic Use
  • Sponsors Viking Therapeutics

    • Most Recent Events

    • 29 Aug 2020 Results of liver fat assessments taken at 16 weeks; 4-weeks post-completion of dosing, presented at The International Liver Congress 2020
    • 28 Aug 2020 According to a Viking Therapeutics media release, data from this study were presented at the Digital International Liver Congress .
    • 28 Aug 2020 Results published in the Viking Therapeutics media release

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